Variant Synonymizer: Platform to identify mutations defined in different ways is available now!

VarSy

Over 2,000 gene–disease validation summaries are now available—no login required!

Browse Summaries

Stats

Total associations
6681
Unique genes
4239
Unique diseases
3297
Gene–disease association summaries

Gene–Disease Browser

Need updated, customized, evidence‑backed summaries? Get it from the leaders in AI‑powered, evidence‑backed summaries provider.
Gene Disease Score Actions
CCL19
(HGNC:10617)
tuberculosis
(MONDO_0018076)
Limited
SF3A1
(HGNC:10765)
colorectal cancer
(MONDO_0005575)
Disputed
SEMA3B
(HGNC:10724)
schizophrenia
(MONDO_0005090)
Limited
BMP8B
(HGNC:1075)
premature menopause
(MONDO_0001119)
Limited
SDC3
(HGNC:10660)
obesity disorder
(MONDO_0011122)
Moderate
SERF1A
(HGNC:10755)
spinal muscular atrophy
(MONDO_0001516)
Disputed
BLMH
(HGNC:1059)
Alzheimer disease
(MONDO_0004975)
Disputed
SAR1B
(HGNC:10535)
chylomicron retention disease
(MONDO_0009528)
Definitive
SCML2
(HGNC:10581)
Nance-Horan syndrome
(MONDO_0010545)
Refuted
CNNM4
(HGNC:105)
Jalili syndrome
(MONDO_0009007)
Definitive
SALL2
(HGNC:10526)
Alport syndrome
(MONDO_0018965)
Disputed
CLEC11A
(HGNC:10576)
acute myeloid leukemia
(MONDO_0018874)
Limited
STMN2
(HGNC:10577)
osteoarthritis
(MONDO_0005178)
Disputed
SARS1
(HGNC:10537)
Charcot-Marie-Tooth disease
(MONDO_0015626)
Moderate
SC5D
(HGNC:10547)
lathosterolosis
(MONDO_0011816)
Moderate
SALL2
(HGNC:10526)
nephrotic syndrome
(MONDO_0005377)
Limited
S100P
(HGNC:10504)
lung cancer
(MONDO_0008903)
Limited
RRAD
(HGNC:10446)
Brugada syndrome
(MONDO_0015263)
Limited
RTN3
(HGNC:10469)
Alzheimer disease
(MONDO_0004975)
Disputed
S100A2
(HGNC:10492)
colorectal cancer
(MONDO_0005575)
Limited
Showing 6641–6660 of 6681